Biodiversity Data Journal :
Taxonomic paper
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Corresponding author:
Academic editor: Bruno Danis
Received: 20 Nov 2015 | Accepted: 19 Jan 2016 | Published: 25 Jan 2016
© 2016 Adrian Glover, Helena Wiklund, Muriel Rabone, Diva Amon, Craig Smith, Tim O'Hara, Christopher Mah, Thomas Dahlgren
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Glover A, Wiklund H, Rabone M, Amon D, Smith C, O'Hara T, Mah C, Dahlgren T (2016) Abyssal fauna of the UK-1 polymetallic nodule exploration claim, Clarion-Clipperton Zone, central Pacific Ocean: Echinodermata. Biodiversity Data Journal 4: e7251. https://doi.org/10.3897/BDJ.4.e7251
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We present data from a DNA taxonomy register of the abyssal benthic Echinodermata collected as part of the Abyssal Baseline (ABYSSLINE) environmental survey cruise ‘AB01’ to the UK Seabed Resources Ltd (UKSRL) polymetallic-nodule exploration claim ‘UK-1’ in the eastern Clarion-Clipperton Zone (CCZ), central Pacific Ocean abyssal plain. Morphological and genetic data are presented for 17 species (4 Asteroidea, 4 Crinoidea, 2 Holothuroidea and 7 Ophiuroidea) identified by a combination of morphological and genetic data. No taxa matched previously published genetic sequences, but 8 taxa could be assigned to previously-described species based on morphology, although here we have used a precautionary approach in taxon assignments to avoid over-estimating species ranges. The Clarion-Clipperton Zone is a region undergoing intense exploration for potential deep-sea mineral extraction. We present these data to facilitate future taxonomic and environmental impact study by making both data and voucher materials available through curated and accessible biological collections.
We present data from a DNA taxonomy register of the abyssal benthic Echinodermata collected as part of the Abyssal Baseline (ABYSSLINE) environmental survey cruise ‘AB01’ to the UK Seabed Resources Ltd (UKSRL) polymetallic-nodule exploration claim ‘UK-1’ in the eastern Clarion-Clipperton Zone (CCZ), central Pacific Ocean (
This paper is the start of an iterative approach to providing regional taxonomic synthesis for a region that is undergoing intense deep-sea mineral exploration for high-grade polymetallic nodules regulated by Sponsoring States (here the United Kingdom Government) and the International Seabed Authority (
The abyssal zone of the world’s oceans has been defined as the seafloor between depths of 3000m and 6000m, a bathymetric zone that encompasses 54% of the geographic surface of the planet (
The Clarion-Clipperton Zone (hereafter, CCZ) is so called as it lies between the Clarion and Clipperton Fracture Zones, topographical highs that extend longitudinally across almost the entire eastern Pacific. There is no strict definition of the region, but it has come to be regarded as the area between these fracture zones that lies within international waters and encompasses the main areas of commercial interest for polymetallic-nodule mining. Areas licensed for mining by the International Seabed Authority (ISA), as well as mining reserve areas and areas protected from mining by the ISA (
The Clarion-Clipperton Zone, central Pacific Ocean (purple box) is a 6 milllion km2 region at the time of writing containing only 290 online-databased records of echinoderm species (
Within the 6 million sq km CCZ, as defined above, current online data sources prior to this publication list only 50 known species of echinoderms from 290 records (
It is widely accepted that knowledge of baseline biodiversity and biogeography in the CCZ is severely hampered by a lack of modern DNA-supported taxonomic studies (
The ABYSSLINE environmental baseline survey includes three 30x30km survey boxes (strata), distributed across the UK-1 claim area, and an additional reference sites outside of the UK-1 claim area (
'UK-1 Stratum A' ABYSSLINE biological baseline survey box sited within the UK-1 polymetallic nodule exploration claim. Stratum A is a 30x30km survey box in the northern sector of the 58,000 km2 claim area. Echinoderm sample localities are indicated by green circles from the AB01 RV Melville survey cruise, October 2013. Inset map A: the site location within the central Pacific, inset map B: all the echinoderm sampling locations (including site 'ROV7' to the west). Both inset maps use GEBCO 2014 bathymetry (global 30 arc-second interval grid data set). Seafloor bathymetry from the RV Melville ABYSSLINE cruise is shown in the main map.
A comprehensive description of our DNA taxonomy pipeline is provided in
ABYSSLINE UK-1 polymetallic nodule exploration claim field pipeline for DNA taxonomy. ABYSSLINE AB01 cruise sampling aboard RV Melville in October 2013. (a) Preparing Box Core (BC) for deployment, (b) BC entering the water, (c) Megacore entering the water, (d-f) Epibenthic Sledge shown on recovery in water and cod-end where samples are taken, (g) controlling BC deployment on seafloor, (h) echosounder trace showing BC approaching seabed reflection, (i) successful BC surface after recovery, 50cm x 50cm, (j) carefully sifting mud in chilled filtered seawater (approx. temp 5-7°C) to remove live animals in undamaged state, (k) live-sorting aboard ship, taking samples for DNA and photomicrographs of specimens down to <1mm in size. All images by Glover, Dahlgren & Wiklund. A more comprehensive description of our methods is provided in
Extraction of DNA was done with DNeasy Blood and Tissue Kit (Qiagen) using a Hamilton Microlab STAR Robotic Workstation. About 1800 bp of 18S, 450 bp of 16S, and 650 bp of cytochrome c oxidase subunit I (COI) were amplified using primers listed in Table
Primer | Sequence 5'-3' | Reference |
18S | ||
18SA | AYCTGGTTGATCCTGCCAGT |
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18SB | ACCTTGTTACGACTTTTACTTCCTC |
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620F | TAAAGYTGYTGCAGTTAAA |
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1324R | CGGCCATGCACCACC |
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COI | ||
LCO1490 | GGTCAACAAATCATAAAGATATTGG |
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HCO2198 | TAAACTTCAGGGTGACCAAAAAATCA |
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polyLCO | GAYTATWTTCAACAAATCATAAAGATATTGG |
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polyHCO | TAMACTTCWGGGTGACCAAARAATCA |
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16S | ||
16SbrH | CCGGTCTGAACTCAGATCACGT |
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Ann16SF | GCGGTATCCTGACCGTRCWAAGGTA |
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Overlapping sequence fragments were merged into consensus sequences using Geneious R6 (www.geneious.com,
The field and laboratory pipelines created a series of databases and sample sets that were then integrated into a data-management pipeline (Fig.
All future studies of biogeographic and bathymetric ranges, gene-flow, extinction risks, natural history, reproductive ecology, functional ecology and geochemical interactions of CCZ species are dependent on accurate identifications faciliated by taxonomy. This taxonomy, presented here, is itself dependent on a sound theoretical underpinning – a species concept - coupled with the availability of both raw data and voucher samples. Here we use a phylogenetic species concept, sensu
The following sections detail the phylogenetic analysis and data resources that underpins the species hypotheses presented in the taxon treatments. A full list of all taxa including Natural History Museum Accession Numbers, NHM Molecular Collection Facility (NHM-MCF) FreezerPro numbers and NCBI GenBank Accession numbers is provided in Table
Taxon treatments presented in this paper. Includes Natural History Museum global unique identifier (GUID) which link to the record in the Museum Data Portal (data.nhm.ac.uk), new NCBI GenBank accession numbers (GenBank#), ABYSSLINE Record number (ABYSSLINE_Record#) and NHM Molecular Collection Facility sample ID number (NHMUK_MCF#). Record numbers include both material archived at NHM (all tissue samples and DNA samples, plus some morphological material including whole specimens for some taxa) and material currently housed at the Craig R Smith lab, University of Hawaii (larger 'megafaunal' material indicated by CS numbers in the ABYSSLINE record#). GenBank numbers for data downloaded from GenBank for phylogenetic analysis are presented in Suppl. material
Class | Morphological identification | GUID | ABYSSLINE_ record# |
NHMUK_ MCF# |
Genbank_ CO1# |
Genbank_ 16S# |
Genbank_ 18S# |
Asteroidea | Asteroidea sp. (NHM_054) | de4bd6ce-07fe-496e-bffc-67a4c6b9782c | NHM_054 | 185546311 | --- | KU519512 | KU519530 |
Asteroidea | Asteroidea sp. (NHM_054) | bc03fc1a-3613-41a2-b1f1-bf905e0fa6d0 | NHM_375 | 185546346 | --- | KU519528 | --- |
Asteroidea | Freyastera cf. benthophila | b7ffe7a2-7be1-4d4f-b784-7aaecf0ee743 | NHM_413 AB01_CS10 | 185546349 | KU519550 | KU519518 | KU519535 |
Asteroidea | Freyastera cf. benthophila | 16599946-2aba-4710-98e6-43c522061878 | NHM_421 | 185546363 | KU519551 | --- | --- |
Asteroidea | Porcellanaster cf. ceruleus | c57f1bd3-1b32-41e6-8e1d-0ad6472e4327 | NHM_168 | 185546321 | KU519568 | --- | --- |
Asteroidea | Porcellanaster cf. ceruleus | 7e8ca2d8-aea1-45bd-b7e0-d0575cadd82d | NHM_200 | 185546325 | KU519569 | --- | --- |
Asteroidea | Porcellanaster cf. ceruleus | 95d0bd7f-0df9-47e4-8003-cd12007d54b4 | NHM_253 | 185546332 | KU519570 | KU519525 | KU519542 |
Asteroidea | Porcellanaster cf. ceruleus | d15a68e0-b2b3-40b4-8cab-0563609cc80d | NHM_267 | 185546329 | KU519571 | --- | --- |
Asteroidea | Porcellanaster cf. ceruleus | 76acc5a2-6e0e-4599-8104-b8e243af10c4 | NHM_408 | 185546348 | KU519572 | --- | --- |
Asteroidea | Styracaster paucispinus | 4ae2430e-549e-47f2-ba5d-0e9a08443d31 | NHM_374 | 185546345 | KU519573 | KU519527 | KU519543 |
Crinoidea | Crinoidea sp. (NHM_008) | b2a871bf-46d5-4639-a839-427a3efa848c | NHM_008 | 185546315 | KU519547 | KU519514 | KU519531 |
Crinoidea | Crinoidea sp. (NHM_055) | 280c758b-5287-4a13-9f45-f6a6150b37d0 | NHM_055 | 185546310 | KU519548 | KU519515 | KU519532 |
Crinoidea | Crinoidea sp. (NHM_056) | 92825c07-a16d-4c5e-a8e9-4fbcdc8cf44a | NHM_056 | 185546309 | --- | KU519516 | KU519533 |
Crinoidea | Crinoidea sp. (NHM_300) | 2866f91e-b99e-4703-a9d3-fe1876df1da1 | NHM_300 | 185546328 | KU519549 | KU519517 | KU519534 |
Holothuroidea | Benthodytes cf. sanguinolenta | d0062182-89dc-4deb-b746-688289783b5f | NHM_216 AB01_CS03 | 185546339 | KU519546 | KU519513 | --- |
Holothuroidea | Psychropotes cf. semperiana | 38c16bec-7bf9-4c2b-b862-5da460ba6c0c | NHM_220 AB01_CS05 | 185546335 | --- | KU519526 | --- |
Ophiuroidea | Amphioplus cf. daleus | 72db478a-ea4f-4f3e-be08-95ec9fb4d20e | NHM_094 | 185546316 | KU519544 | --- | --- |
Ophiuroidea | Amphioplus cf. daleus | 15e6ddc7-3ca7-453c-bba5-f84888716505 | NHM_447 AB01_CS15 | 185546357 | KU519545 | KU519511 | KU519529 |
Ophiuroidea | Ophiomusium cf. glabrum | c1c4d8f3-6cd5-439f-a546-943b5e2e8d8f | NHM_009 | 185546314 | KU519552 | --- | --- |
Ophiuroidea | Ophiomusium cf. glabrum | 4d6f6aaf-93fd-4629-b224-2ce8dd3320f6 | NHM_124 AB01_CS02 | 185546319 | KU519553 | --- | --- |
Ophiuroidea | Ophiomusium cf. glabrum | 2ed865af-1605-4d78-8fd8-9c7659781854 | NHM_256 | 185546331 | KU519554 | --- | --- |
Ophiuroidea | Ophiomusium cf. glabrum | 11948cb9-654f-4519-a654-f134380093ea | NHM_329 AB01_CS06 | 185546341 | KU519555 | KU519519 | KU519536 |
Ophiuroidea | Ophiomusium cf. glabrum | 292bd655-83d6-440f-9668-82dfa4185b04 | NHM_335 | 185546342 | KU519556 | --- | --- |
Ophiuroidea | Ophiomusium cf. glabrum | 68072fc9-3e84-4202-8e97-6c9c0c5fc83d | NHM_415 AB01_CS12 | 185546351 | KU519557 | --- | --- |
Ophiuroidea | Ophiomusium cf. glabrum | 5ad996fe-134a-4625-a404-9d0cdae435d4 | NHM_452 | 185546352 | KU519558 | --- | --- |
Ophiuroidea | Ophiotholia sp. (NHM_076) | bd6fe2ce-b4ae-470e-8bdc-cf28a94c6208 | NHM_076 | 185546306 | KU519559 | KU519520 | KU519537 |
Ophiuroidea | Ophiotholia sp. (NHM_076) | 97d40306-fe6c-4911-8e68-1f9efc3d838f | NHM_078 | 185546305 | KU519560 | --- | --- |
Ophiuroidea | Ophiotholia sp. (NHM_076) | 479218ae-813b-4736-b3f2-7eec63640ffd | NHM_104 | 185546317 | KU519561 | --- | --- |
Ophiuroidea | Ophiotholia sp. (NHM_076) | 90e22ace-ef5d-4cb5-a4a5-29fcd55ed660 | NHM_119 | 185546318 | KU519562 | --- | --- |
Ophiuroidea | Ophiuroidea incertae sedis sp. (NHM_041) | 608349ff-5adf-4e1e-8cd7-7e0e41aee222 | NHM_041 | 185546312 | KU519563 | KU519521 | KU519538 |
Ophiuroidea | Ophiuroidea incertae sedis sp. (NHM_072) | 241d094a-568f-4194-997c-fd08f67dcdac | NHM_072 | 185546307 | KU519564 | KU519522 | KU519539 |
Ophiuroidea | Ophiuroidea incertae sedis sp. (NHM_303) | e9f38ce3-5ed5-49f3-8713-c26de2eefd2b | NHM_303 | 185546340 | KU519565 | KU519523 | KU519540 |
Ophiuroidea | Ophiuroidea incertae sedis sp. (NHM_303) | 93b0a70d-c74e-4735-b70e-0c6e4c6a36ff | NHM_371 | 185546344 | KU519566 | --- | --- |
Ophiuroidea | Perlophiura profundissima | f263bc90-6307-462c-9e02-7b87d20e2840 | NHM_257 | 185546330 | KU519567 | KU519524 | KU519541 |
Phylogenetic analysis of the Asteroidea (Fig.
Phylogenetic analysis of the Crinoidea (Fig.
Phylogenetic analysis of the Holothuroidea (Fig.
Phylogenetic analysis of the Ophiuroidea (Fig.
Voucher material NHM_54, width of disc 4.7mm. Arms absent. Medial antenna absent (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Morphologically and genetically close to Eremicaster sp (Fig.
15cm long arm fragments of a Freyellidae recovered from ROV biobox. Identified by DNA and morphological examination (Fig.
Freyastera cf. benthophila Sladen, 1899. (a) Specimen NHM_413 (arm fragment) being recovered in situ from the seafloor during ROV dive RV06, (b) Additional, unsampled specimen, imaged during AB01 video survey and identified based on imagery as the same species, (c) Tentacle of specimen NHM_413 only part recovered; inset shows detail of tentacle. Scale bars (b) laser dots 242mm apart, (c) 20mm. Image attribution (a) Smith & Amon 2013, (c) Glover, Dahlgren & Wiklund 2015.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens (Fig.
Voucher material NHM_267 maximum width of disc 10.5mm (Fig. 11). Length of medial antenna 3.1mm- specimen NHM_253 (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Morphologically matches diagnosis of Porcellanaster ceruleus Wyville Thomson, 1877. Forms a unique monophyletic clade distinct from other AB01 specimens. Sequences of this material has no genetic matches on GenBank or Barcode of Life Database. The type material of Porcellanaster ceruleus Wyville Thomson, 1877 was dredged by the Challanger SE of New York (38°34'N; 72°10'W, 2270m depth) wich is significantly separated from our collection site. We assign the tentative name Porcellanaster cf. ceruleus to this material until we have a better understanding of genetic variation within the species including data from the type locality.
Voucher material NHM_374, width of disc 8.2mm, maximum width of specimen including arms 16.5mm (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Morphologically matches diagnosis of Styracaster paucispinus based on descriptions in
Calyx 1.5mm long and 1.4mm wide with arms possibly incomplete. Arms present with 0.24mm in width, 0.95mm in length. Total length of calyx and distal part of stalk preserved 6.5mm. Stalk 0.32mm in width, stalk columnals approx 1mm in length. (Fig.
Crinoidea sp. Specimen NHM_008. (a) Specimen attached to polymetallic nodule, live photograph, after recovery from box core. (b) Preserved specimen following DNA extraction. (c) Detail of crown, calyx and basals. Scale bars (a) 3mm, (b) 1mm, (c) 0.5mm. Image attribution Glover, Dahlgren & Wiklund 2015.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Morphologically close to Hyocrinus foelli
Specimen observed live on a small potato-sized polymetallic nodule from the eastern CCZ abyssal plain.
Specimen including stalk and crown, calyx with arms, 8mm in total length, 5 arms, 0.31mm in width, as present in original specimen, prior to DNA sampling, with length 1.3mm from distal portion of calyx. Distally, pinnules observed on arms (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. No genetic matches on GenBank or Barcode of Life Database.
Found living on polymetallic nodule.
Specimen including stalk and crown, calyx with proximal arms only, 5mm in total length. Calyx 0.62mm in width, including proximal arms 0.86mm in length. Distally, pinnules observed on arms arising laterally from arms (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. No genetic matches on GenBank or Barcode of Life Database.
Found on polymetallic nodule.
Specimen lacks calyx, crown, arms. Stalk 6.5mm in length, attached to nodule fragment. Columnals 1.6mm in length, 0.28mm in width (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. No genetic matches on GenBank or Barcode of Life Database. Lacks crown and calyx.
Found on polymetallic nodule.
Morphologically agrees with either Benthodytes sanguinolenta or Benthodytes typica both from
Benthodytes cf. sanguinolenta Théel, 1882. Specimen NHM_216. (a) Specimen NHM_216 in situ on seafloor shortly before collection by ROV manipulator arm, (b) Live specimen photographed immediately after recovery from the ROV biobox, upper (dorsal view), lower (ventral view). Scale bar 5cm. Image attribution (a) Smith & Amon 2013, (b) Glover, Dahlgren & Wiklund, 2015.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens and no match (16S) to any GenBank or BOLD databases. Morphologically consistent with Benthodytes sanguinolenta or B. typica. The type locality of B. sanguinolenta is in the Pacific ocean (34°7'S; 73°56'W, 4000m depth) while type locality of B. typica is Atlantic (35°47'N; 8°23'W, 2000m depth) (
Observed moving on the seabed amongst polymetallic nodules.
Distinctive large holothurian with sail, close morphological match to Psychropotes semperiana from
Psychropotes cf. semperiana Théel, 1882. Specimen NHM_220. (a) Live specimen photographed in-situ on the seafloor. (b) Same specimen dorsal view after recovery by ROV imaged underwater in cold-water tank. (c) Ventral view. Scale bars (c) 10cm. Image attribution (a) Smith & Amon 2013, (b) Glover, Dahlgren & Wiklund, 2015.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens and no match to any GenBank or BOLD databases. Morphologically consistent with Psychropotes semperiana Théel, 1882. The type locality of Psychropotes semperiana is Atlantic (5°48'N; 14°20'W, 4500m depth) and we use the tentative name Psychropotes cf. semperiana for this material until we have a better understanding of genetic variation within the species including data from the type locality.
Observed moving on the seabed amongst polymetallic nodules.
Voucher material recovered from megacore sample, specimen with disc of 1cm diameter (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically consistent with Amphioplus (Unioplus) daleus
Recovered from a range of sampling gears, NHM_447 recovered alive in top of multiple core tube.
Voucher material, NHM_329, disc approx 20mm in diameter. Additional voucher material (12 specimens) ranges in size from 2mm to 20mm in diameter (Fig.
Ophiomusium cf. glabrum Lütken and Mortensen, 1899. (a) Voucher material Specimen NHM_329 with insets showing detail of dorsal and ventral surface of disc. (b) NHM_124. (c) NHM_256. (d) NHM_338. (e) Unsampled specimens of suspected O. cf glabrum imaged during ROV surveys, showing 1 specimen on sediment surface and 1 specimen partially buried in sediment (green dot is a laser scale marker, cropped here). All voucher material specimens and designations confirmed with DNA data. Scale bars (a) 20mm, (g) 2mm. Image attribution (a-d) Glover, Dahlgren & Wiklund 2015 (e) Smith & Amon 2013.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically fits Ophiomusium cf. glabrum detailed in (
The most abundant brittle-star in the UK-1 exploration claim survey box UK-1 Stratum A, frequently observed by the ROV on the sediment surface and on nodules.
Voucher material, consisting of a series of fragments of arms and one partial disc. All material specimens form a monophyletic clade based on DNA. Arm processes (parasols) suggestive of Ophiotholia sp affinity. In NHM_076, arms are 0.31mm wide, with parasol-shaped processes of 0.19mm in length, parasols, 0.048mm in width (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically perhaps close to Ophiotholia but requires further sampling.
Specimens recovered from two box cores, two specimens from each. Specimens from the same box cores genetically identical, so could be fragments of the same species.
Small disc fragments found in several samples, distinct petal arrangement visible ventrally (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically not recognisable.
Small fragment consisting of orange-coloured disc, arms absent or missing (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically not recognisable.
Small fragments found in several samples, distinct upturned arms and prounonced hump on crest (Fig.
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically not recognisable.
Specimen examined and matches Perlophiura profundissima Belyaev and Litvinova, 1972 (
Genetic data for this taxa with new GenBank accession numbers are provided in Table
Forms a unique monophyletic clade distinct from other AB01 specimens. Morphologically agrees with Perlophiura profundissima but no genetic data available from type locality or any location for this taxon but type locality appears to be North Pacific at abyssal depths (
Within the entire 6 million sq km Clarion Clipperton Zone, the best current online databases (
It is noteworthy that there was not a single 100% match for any of our sequences obtained with data on either NCBI GenBank or BOLD databases (
The lack of comparative genetic data also has implications for our understanding of species ranges. We know that cryptic diversity is common in the deep sea (
The increased activity in terms of research cruises and sample collection in the CCZ make it more important than ever to provide taxonomic data quickly for an iterative building of baseline biodiversity knowledge in the CCZ region. Making these data available through rapid publication in open-access journals that support data-aggregator online systems is a key first step in this process.
The ABYSSLINE (ABYSSal baseLINE) environmental survey of the UK-1 exploration claim is supported by a collaborative partnership between 6 non-profit global academic research institutes (University of Hawaii at Manoa, Natural History Museum, Uni Research, National Oceanography Centre, Senckenberg Institute, IRIS Norway) and through a commercial arrangement with UK Seabed Resources Ltd. Additional support was provided by the Swedish research council FORMAS (TGD). We would like to acknowledge the support of Magdalena Georgieva from the Natural History Museum team in sampling on board ship. We would particularly like to acknowledge the expert support from the Senckenberg Institute team in the deployment and recovery of successful Brenke Epibenthic Sledge samples (Nils Brenke, Pedro Martinez and Inga Morhbeck). We would like to acknowledge the support of the entire scientific party and the Masters and Crew of the Research Vessel Melville during the first cruise of the ABYSSLINE project in October 2013. Thanks also to Jackie Mackenzie-Dodds & Chiho Ikebe (Molecular Collection Facility, NHM).
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Data were provided by all the authors. The manuscript was first drafted by AGG and subsequently edited by all the authors.
List of taxa downloaded from GenBank that are included in the phylogenetic analyses, with their Genbank accession numbers. Accession numbers for taxa sequenced in this study are found in Table 2.